TY - JOUR
T1 - Survival of patients with advanced metastatic melanoma
T2 - The impact of MAP kinase pathway inhibition and immune checkpoint inhibition - Update 2019
AU - Ugurel, Selma
AU - Röhmel, Joachim
AU - Ascierto, Paolo A.
AU - Becker, Jürgen C.
AU - Flaherty, Keith T.
AU - Grob, Jean J.
AU - Hauschild, Axel
AU - Larkin, James
AU - Livingstone, Elisabeth
AU - Long, Georgina V.
AU - Lorigan, Paul
AU - McArthur, Grant A.
AU - Ribas, Antoni
AU - Robert, Caroline
AU - Zimmer, Lisa
AU - Schadendorf, Dirk
AU - Garbe, Claus
N1 - Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2020/5/1
Y1 - 2020/5/1
N2 - Background: Recent therapeutic strategies, particularly MAP kinase pathway inhibitors (BRAF, MEK) and immune checkpoint blockers (CTLA-4, PD-1), have been put on the test for their differential impact on long-term survival of metastatic melanoma patients. Various agents, dose regimens and combinations have been tested against each other vigorously within these two therapy groups. However, results from prospective head-to-head comparative trials comparing both strategies against each other are still lacking. Methods: We performed an exploratory analysis of survival data from selected clinical trials representative for these two treatment strategies in advanced metastatic melanoma. 84 Kaplan–Meier survival curves from 26 trials were digitised and grouped by therapy strategy and treatment line. For each of these groups, mean survival curves were generated for progression-free (PFS) and overall survival (OS) by weighted averaging. Results: Survival curves grouped together by therapy strategy revealed a high concordance, with a larger extent in the first-line setting compared to higher treatment lines. In first-line therapy, the averaged 3-year OS proportions were 41.3% for BRAF plus MEK inhibition, 49.9% for PD-1 inhibition, and 58.4% for CTLA-4 plus PD-1 inhibition. Comparison of the mean PFS and OS curves of kinase inhibition and checkpoint blockade revealed a superiority of combined BRAF plus MEK inhibition within the first 12 months, later changing to a superiority of PD-1 blockers alone or in combination with CTLA-4 blockade. In second-line or higher, BRAF plus MEK inhibition was superior to anti-PD-1 monotherapy throughout the first three years; averaged 3-year OS proportions were 42.4% for BRAF plus MEK inhibition, and 40.1% for PD-1 inhibition. Conclusions: and relevance: These results need confirmation by head-to-head comparative randomised clinical trials.
AB - Background: Recent therapeutic strategies, particularly MAP kinase pathway inhibitors (BRAF, MEK) and immune checkpoint blockers (CTLA-4, PD-1), have been put on the test for their differential impact on long-term survival of metastatic melanoma patients. Various agents, dose regimens and combinations have been tested against each other vigorously within these two therapy groups. However, results from prospective head-to-head comparative trials comparing both strategies against each other are still lacking. Methods: We performed an exploratory analysis of survival data from selected clinical trials representative for these two treatment strategies in advanced metastatic melanoma. 84 Kaplan–Meier survival curves from 26 trials were digitised and grouped by therapy strategy and treatment line. For each of these groups, mean survival curves were generated for progression-free (PFS) and overall survival (OS) by weighted averaging. Results: Survival curves grouped together by therapy strategy revealed a high concordance, with a larger extent in the first-line setting compared to higher treatment lines. In first-line therapy, the averaged 3-year OS proportions were 41.3% for BRAF plus MEK inhibition, 49.9% for PD-1 inhibition, and 58.4% for CTLA-4 plus PD-1 inhibition. Comparison of the mean PFS and OS curves of kinase inhibition and checkpoint blockade revealed a superiority of combined BRAF plus MEK inhibition within the first 12 months, later changing to a superiority of PD-1 blockers alone or in combination with CTLA-4 blockade. In second-line or higher, BRAF plus MEK inhibition was superior to anti-PD-1 monotherapy throughout the first three years; averaged 3-year OS proportions were 42.4% for BRAF plus MEK inhibition, and 40.1% for PD-1 inhibition. Conclusions: and relevance: These results need confirmation by head-to-head comparative randomised clinical trials.
KW - Immune checkpoint blockers
KW - Kinase inhibitors
KW - Melanoma
KW - Survival
KW - Therapy
UR - http://www.scopus.com/inward/record.url?scp=85081238037&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2020.02.021
DO - 10.1016/j.ejca.2020.02.021
M3 - Article
C2 - 32179447
AN - SCOPUS:85081238037
SN - 0959-8049
VL - 130
SP - 126
EP - 138
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -